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FDA 510(k)

VARILIFT-L INTERBODY FUSION DEVICE

K-Number: K131296 · 2013-09-03

ApplicantWenzel Spine, Inc.
Decision Date2013-09-03
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VARILIFT-L INTERBODY FUSION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Wenzel Spine, Inc.. It received FDA 510(k) clearance on 2013-09-03 under 510(k) number K131296. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARILIFT-L INTERBODY FUSION DEVICE?

VARILIFT-L INTERBODY FUSION DEVICE is a medical device that received FDA 510(k) clearance on 2013-09-03. The listed applicant is Wenzel Spine, Inc.. The 510(k) number is K131296.

When did VARILIFT-L INTERBODY FUSION DEVICE receive FDA 510(k) clearance?

VARILIFT-L INTERBODY FUSION DEVICE received FDA 510(k) clearance on 2013-09-03, under 510(k) number K131296.

Who is the listed applicant for VARILIFT-L INTERBODY FUSION DEVICE?

The FDA 510(k) record lists Wenzel Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARILIFT-L INTERBODY FUSION DEVICE?

The FDA product code for VARILIFT-L INTERBODY FUSION DEVICE is MAX.

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Other records listing Wenzel Spine, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262595VariLift-C Cervical Interbody Fusion SystemK250247panaSIa SI Fusion SystemK231076VariLift®-C Interbody Fusion SystemK231807primaLOK™ SP Interspinous Fusion SystemK180822VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System

Related Devices (Code: MAX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261049SCALA® TLSpineart SAK261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SySeaSpine Orthopedics CorporationK253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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